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NCT01440972 · ClinicalTrials.gov registry record · NA
Assessment of Efficacy of Low Intensity Resistance Training in Women at Risk for Symptomatic Knee Osteoarthritis
A NA study, sponsored by University of Iowa.
- Completed
- Registry status
- NA
- Development phase
- 45
- Enrollment target
NCT01440972 is a NA study that has completed, run by University of Iowa. The registered enrollment target is 45 participants.
The verdict
NCT01440972, a NA study, has completed, sponsored by University of Iowa.
- COMPLETED
- Registry status
- NA
- Development phase
- 45 participants
- Enrollment target
Study Summary
The purpose of this study is to asses the efficacy of a 4 week low-intensity resistance training program with concurrent application of partial blood flow restriction (PBFR) to the exercising limbs to improve quadriceps strength and size, leg muscle power, and mobility in women at risk for developing symptomatic knee osteoarthritis. The primary outcome will be change in isotonic double leg-press 1 repetition maximum (1RM) strength. The investigators will test the following hypotheses. In comparison with low-intensity resistance training without use of PBFR, a four-week low-intensity resistance-training program with PBFR will: Primary Hypothesis: Increase (a) double leg-press 1RM strength and (b) isokinetic knee extensor strength Secondary Hypotheses: 1. Increase quadriceps muscle volume assessed by MRI 2. Increase lower limb muscle power on (a) double leg-press at 40% 1RM and (b) a timed stair climb 3. Not adversely effect knee pain or quality of life assessed by the Knee injury and Osteoarthritis Outcome Score (KOOS) questionnaire
Interventions
- OTHER partial blood flow restriction (PBFR)
- OTHER low intensity resistance training
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 45 participants |
| Start Date | 2011-09 |
| Est. Completion | 2011-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01440972
The ClinicalTrials.gov registry entry for NCT01440972 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Iowa, which has 228 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which partial blood flow restriction (PBFR) is the first listed.
NCT01440972 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01440972 about?
NCT01440972 is a clinical study titled "Assessment of Efficacy of Low Intensity Resistance Training in Women at Risk for Symptomatic Knee Osteoarthritis". The purpose of this study is to asses the efficacy of a 4 week low-intensity resistance training program with concurrent application of partial blood flow restriction (PBFR) to the exercising limbs to improve quadriceps strength and size, leg muscle power, and mobility in women at risk for developin...
What is the current status of trial NCT01440972?
This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2011-09. Estimated completion is 2011-11.
What interventions are being tested in trial NCT01440972?
The interventions under investigation include: partial blood flow restriction (PBFR) (OTHER), low intensity resistance training (OTHER).
Who is sponsoring clinical trial NCT01440972?
This trial is sponsored by University of Iowa, which has 228 total clinical trials registered on ClinicalTrials.gov.
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